Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers

Benjamin White,1 Anna Evison,1 Eszter Dombi,1 Helen E Townley1,2 1Nuffield Department of Obstetrics and Gynaecology, Women’s Centre, John Radcliffe Hospital, 2Department of Engineering Science, Oxford University, Oxford, UK Abstract: Rhabdomyosarcoma (RMS) is the most common soft tissue sa...

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Autores principales: White B, Evison A, Dombi E, Townley HE
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Publicado: Dove Medical Press 2017
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spelling oai:doaj.org-article:a7e9bf07be644b07993056d6c9e973a82021-12-02T03:50:36ZImproved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers1177-8903https://doaj.org/article/a7e9bf07be644b07993056d6c9e973a82017-12-01T00:00:00Zhttps://www.dovepress.com/improved-delivery-of-the-anticancer-agent-citral-using-bsa-nanoparticl-peer-reviewed-article-NSAhttps://doaj.org/toc/1177-8903Benjamin White,1 Anna Evison,1 Eszter Dombi,1 Helen E Townley1,2 1Nuffield Department of Obstetrics and Gynaecology, Women’s Centre, John Radcliffe Hospital, 2Department of Engineering Science, Oxford University, Oxford, UK Abstract: Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children, with a 5-year survival rate of between 30 and 65%. Standard treatment involves surgery, radiation treatment, and chemotherapy. However, there is a high recurrence rate, particularly from locoregional spread. We investigated the use of the natural compound citral (3,7-dimethyl-2,6-octadienal), which can be found in a number of plants, but is particularly abundant in lemon grass (Cymbopogon citratus) oil, for activity against immortalized RMS cells. Significant cancer cell death was seen at concentrations above 150 μM citral, and mitochondrial morphological changes were seen after incubation with 10 μM citral. However, since citral is a highly volatile molecule, we prepared albumin particles by a desolvation method to encapsulate citral, as a means of stabilization. We then further incorporated the loaded nanoparticles into a biodegradable polyanhydride wafer to generate a slow release system. The wafers were shown to degrade by 50% over the course of 25 days and to release the active compound. We therefore propose the use of the citral-nanoparticle-polymer wafers for implantation into the tumor bed after surgical removal of a sarcoma as a means to control locoregional spread due to any remaining cancerous cells. Keywords: citral, nanoparticle, wafer, biodegradable, mitochondria, toroidal, cancer, rhabdomyosarcoma, Cymbopogon citratusWhite BEvison ADombi ETownley HEDove Medical PressarticleMedical technologyR855-855.5Chemical technologyTP1-1185ENNanotechnology, Science and Applications, Vol Volume 10, Pp 163-175 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medical technology
R855-855.5
Chemical technology
TP1-1185
spellingShingle Medical technology
R855-855.5
Chemical technology
TP1-1185
White B
Evison A
Dombi E
Townley HE
Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers
description Benjamin White,1 Anna Evison,1 Eszter Dombi,1 Helen E Townley1,2 1Nuffield Department of Obstetrics and Gynaecology, Women’s Centre, John Radcliffe Hospital, 2Department of Engineering Science, Oxford University, Oxford, UK Abstract: Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children, with a 5-year survival rate of between 30 and 65%. Standard treatment involves surgery, radiation treatment, and chemotherapy. However, there is a high recurrence rate, particularly from locoregional spread. We investigated the use of the natural compound citral (3,7-dimethyl-2,6-octadienal), which can be found in a number of plants, but is particularly abundant in lemon grass (Cymbopogon citratus) oil, for activity against immortalized RMS cells. Significant cancer cell death was seen at concentrations above 150 μM citral, and mitochondrial morphological changes were seen after incubation with 10 μM citral. However, since citral is a highly volatile molecule, we prepared albumin particles by a desolvation method to encapsulate citral, as a means of stabilization. We then further incorporated the loaded nanoparticles into a biodegradable polyanhydride wafer to generate a slow release system. The wafers were shown to degrade by 50% over the course of 25 days and to release the active compound. We therefore propose the use of the citral-nanoparticle-polymer wafers for implantation into the tumor bed after surgical removal of a sarcoma as a means to control locoregional spread due to any remaining cancerous cells. Keywords: citral, nanoparticle, wafer, biodegradable, mitochondria, toroidal, cancer, rhabdomyosarcoma, Cymbopogon citratus
format article
author White B
Evison A
Dombi E
Townley HE
author_facet White B
Evison A
Dombi E
Townley HE
author_sort White B
title Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers
title_short Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers
title_full Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers
title_fullStr Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers
title_full_unstemmed Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers
title_sort improved delivery of the anticancer agent citral using bsa nanoparticles and polymeric wafers
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/a7e9bf07be644b07993056d6c9e973a8
work_keys_str_mv AT whiteb improveddeliveryoftheanticanceragentcitralusingbsananoparticlesandpolymericwafers
AT evisona improveddeliveryoftheanticanceragentcitralusingbsananoparticlesandpolymericwafers
AT dombie improveddeliveryoftheanticanceragentcitralusingbsananoparticlesandpolymericwafers
AT townleyhe improveddeliveryoftheanticanceragentcitralusingbsananoparticlesandpolymericwafers
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